A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182056



Internal ID20749096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58325501..58328700hg38UCSC Ensembl
chr13:58899635..58902834hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer